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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 10001 - 10025 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00010001Methylmalonic acidJsmolCC(C(O)=O)C(O)=OUnderivatized118.0266Semi standard non polar1146.1722
RI00010002Phenylpyruvic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C(=O)CC1=CC=CC=C1TMS236.0869Semi standard non polar1517.1733
RI00010003Phenylpyruvic acid,1TMS,isomer#2JsmolC[Si](C)(C)OC(=CC1=CC=CC=C1)C(=O)OTMS236.0869Semi standard non polar1669.7083
RI00010004Phenylpyruvic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C(=O)CC1=CC=CC=C1TBDMS278.1338Semi standard non polar1747.8918
RI00010005Phenylpyruvic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=CC1=CC=CC=C1)C(=O)OTBDMS278.1338Semi standard non polar1924.258
RI00010006Phenylpyruvic acidJsmolOC(=O)C(=O)CC1=CC=CC=C1Underivatized164.0473Standard polar2649.3232
RI00010007Phenylpyruvic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C(=CC1=CC=CC=C1)O[Si](C)(C)CTMS308.1264Standard non polar1695.1923
RI00010008Phenylpyruvic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C(=CC1=CC=CC=C1)O[Si](C)(C)C(C)(C)CTBDMS392.2203Standard non polar2101.561
RI00010009Phenylpyruvic acidJsmolOC(=O)C(=O)CC1=CC=CC=C1Underivatized164.0473Standard non polar1265.6979
RI00010010Phenylpyruvic acidJsmolOC(=O)C(=O)CC1=CC=CC=C1Underivatized164.0473Semi standard non polar1384.9937
RI00010011Phenylpyruvic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C(=CC1=CC=CC=C1)O[Si](C)(C)CTMS308.1264Semi standard non polar1615.4703
RI00010012Phenylpyruvic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C(=CC1=CC=CC=C1)O[Si](C)(C)C(C)(C)CTBDMS392.2203Semi standard non polar2099.9011
RI00010013Phenylpyruvic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C(=CC1=CC=CC=C1)O[Si](C)(C)CTMS308.1264Standard polar1898.3824
RI00010014Phenylpyruvic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C(=CC1=CC=CC=C1)O[Si](C)(C)C(C)(C)CTBDMS392.2203Standard polar2186.295
RI00010015N6-Acetyl-L-lysine,1TMS,isomer#1JsmolCC(=O)NCCCC[C@H](N)C(=O)O[Si](C)(C)CTMS260.1556Semi standard non polar1829.2021
RI00010016N6-Acetyl-L-lysine,1TMS,isomer#2JsmolCC(=O)NCCCC[C@H](N[Si](C)(C)C)C(=O)OTMS260.1556Semi standard non polar1903.0305
RI00010017N6-Acetyl-L-lysine,1TMS,isomer#3JsmolCC(=O)N(CCCC[C@H](N)C(=O)O)[Si](C)(C)CTMS260.1556Semi standard non polar1877.1987
RI00010018N6-Acetyl-L-lysine,1TBDMS,isomer#1JsmolCC(=O)NCCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)CTBDMS302.2026Semi standard non polar2103.4568
RI00010019N6-Acetyl-L-lysine,1TBDMS,isomer#2JsmolCC(=O)NCCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)OTBDMS302.2026Semi standard non polar2168.1458
RI00010020N6-Acetyl-L-lysine,1TBDMS,isomer#3JsmolCC(=O)N(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)CTBDMS302.2026Semi standard non polar2090.764
RI00010021N6-Acetyl-L-lysineJsmolCC(=O)NCCCC[C@H](N)C(O)=OUnderivatized188.1161Standard polar2661.851
RI00010022N6-Acetyl-L-lysine,2TMS,isomer#1JsmolCC(=O)NCCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS332.1951Standard non polar1922.8335
RI00010023N6-Acetyl-L-lysine,2TMS,isomer#2JsmolCC(=O)N(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)CTMS332.1951Standard non polar1945.9568
RI00010024N6-Acetyl-L-lysine,2TMS,isomer#3JsmolCC(=O)N(CCCC[C@H](N[Si](C)(C)C)C(=O)O)[Si](C)(C)CTMS332.1951Standard non polar1942.806
RI00010025N6-Acetyl-L-lysine,2TMS,isomer#4JsmolCC(=O)NCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS332.1951Standard non polar1967.0247
Displaying retention index compounds 10001 - 10025 of 1722868 in total